Ciprofloxacin
- Product NDC
- 0378-1743
- 11-digit product format
- 003781743
- Labeler code
- 0378
- Product ID
- 0378-1743_c4878a00-bb7e-4739-b965-0ba076a5d944
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA078183
- Marketing category
- ANDA
- Marketing start
- 2007-03-22
- Marketing end
- 2020-01-31
- Substance
- CIPROFLOXACIN HYDROCHLORIDE; CIPROFLOXACIN
- Active strength
- 288 mg/1; mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS],Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record